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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863830Generated: October 30, 2026

2-Chlorobenzoxazole → 4-(Benzoxazol-2-yl)benzyl alcohol

https://huagongshe.com/reaction/863830

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzoxazoleHCID 11986—
Reactant4-Bromobenzyl alcoholHCID 70119—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product4-(Benzoxazol-2-yl)benzyl alcoholHCID 15389017—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To 500 ml THF cooled to -78° C. is added butyl lithium (2 eq.) followed by 4-bromobenzyl alcohol (27.2 g; 145 mmol) slowly over 45 minutes in a solution of THF (100 ml) keeping the temperature below -72° C. After 10 minutes following the final addition of the alcohol is added 2-chlorobenzoxazole (23.3 g; 145 mmol) in 25 ml THF slowly over 45 minutes. The temperature is maintained at -78° C. for 1 hour and then warmed to -40° C. for 15 minutes. The reaction is then quenched with 15 ml of acetic acid and allowed to warm to room temperature, diluted with 800 ml ether, washed 3× with H2O and brine, dried (MgSO4) and concentrated in vacuo to obtain a brown oily solid which is washed with 400 ml petroleum ether and filtered to obtain 4-(benzoxazol-2-yl)benzyl alcohol as a tan solid which is used directly in Step B.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05561143
Source datasetuspto-grants-1996_10
ORD IDord-0faeb24169b14b71b4e23f0df636862f
Source noteuspto-grants-1996_10